Canonical Allele Identifier: CA1430244757
Gene: OPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193643391A= , CM000665.2:g.193643391A= GRCh38
NC_000003.11:g.193361180A= , CM000665.1:g.193361180A= GRCh37
NC_000003.10:g.194843874A= NCBI36
NG_011605.1:g.55248A= , LRG_337:g.55248A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361510.8:c.1324A= MANE Select ENSP00000355324.2:p.Lys442=
ENST00000361828.7:c.1159A= ENSP00000354429.3:p.Lys387=
ENST00000361908.8:c.1270A= ENSP00000354681.3:p.Lys424=
ENST00000392436.7:c.1159A= ENSP00000376231.3:p.Lys387=
ENST00000392437.6:c.1213A= ENSP00000376232.2:p.Lys405=
ENST00000642289.1:c.1098A=
ENST00000642445.1:c.1159A= ENSP00000495535.1:p.Lys387=
ENST00000642593.1:c.1159A= ENSP00000494273.1:p.Lys387=
ENST00000643329.1:c.841A= ENSP00000493673.1:p.Lys281=
ENST00000643737.1:c.*1240A= ENSP00000494210.1:n.*1240A=
ENST00000644595.1:c.1159A= ENSP00000494121.1:p.Lys387=
ENST00000644629.1:c.819A=
ENST00000644841.1:c.787A= ENSP00000493988.1:p.Lys263=
ENST00000644959.1:c.1128A=
ENST00000645553.1:c.1174A= ENSP00000494725.1:p.Lys392=
ENST00000646085.1:c.*637A= ENSP00000494509.1:n.*637A=
ENST00000646277.1:c.1324A= ENSP00000495289.1:p.Lys442=
ENST00000646544.1:c.147A=
ENST00000646699.1:c.1098A=
ENST00000646793.1:c.1051A= ENSP00000494512.1:p.Lys351=
ENST00000361150.6:c.1162A= ENSP00000354781.2:p.Lys388=
ENST00000361510.6:c.1324A= ENSP00000355324.2:p.Lys442=
ENST00000361715.6:c.1216A= ENSP00000355311.2:p.Lys406=
ENST00000361828.6:c.1213A= ENSP00000354429.2:p.Lys405=
ENST00000361908.7:c.1270A= ENSP00000354681.3:p.Lys424=
ENST00000392438.7:c.1159A= ENSP00000376233.3:p.Lys387=
ENST00000475899.1:n.355A=
NM_015560.2:c.1159A= , LRG_337t1:c.1159A= NP_056375.2:p.Lys387=
NM_130831.2:c.1051A= NP_570844.1:p.Lys351=
NM_130832.2:c.1105A= NP_570845.1:p.Lys369=
NM_130833.2:c.1162A= NP_570846.1:p.Lys388=
NM_130834.2:c.1213A= NP_570847.2:p.Lys405=
NM_130835.2:c.1216A= NP_570848.1:p.Lys406=
NM_130836.2:c.1270A= NP_570849.2:p.Lys424=
NM_130837.2:c.1324A= , LRG_337t2:c.1324A= NP_570850.2:p.Lys442=
XM_011512863.1:c.1324A= XP_011511165.1:p.Lys442=
XM_011512864.1:c.1270A= XP_011511166.1:p.Lys424=
XM_011512865.1:c.1213A= XP_011511167.1:p.Lys405=
XM_011512866.1:c.1162A= XP_011511168.1:p.Lys388=
XM_011512867.1:c.1159A= XP_011511169.1:p.Lys387=
XM_011512868.1:c.1051A= XP_011511170.1:p.Lys351=
XM_011512869.1:c.1324A= XP_011511171.1:p.Lys442=
NM_001354663.1:c.790A= NP_001341592.1:p.Lys264=
NM_001354664.1:c.787A= NP_001341593.1:p.Lys263=
XR_001740158.2:n.1553A=
XR_001740159.2:n.1388A=
NM_001354663.2:c.790A= NP_001341592.1:p.Lys264=
NM_001354664.2:c.787A= NP_001341593.1:p.Lys263=
NM_130831.3:c.1051A= NP_570844.1:p.Lys351=
NM_130832.3:c.1105A= NP_570845.1:p.Lys369=
NM_130834.3:c.1213A= NP_570847.2:p.Lys405=
NM_130836.3:c.1270A= NP_570849.2:p.Lys424=
NM_015560.3:c.1159A= NP_056375.2:p.Lys387=
NM_130833.3:c.1162A= NP_570846.1:p.Lys388=
NM_130835.3:c.1216A= NP_570848.1:p.Lys406=
NM_130837.3:c.1324A= MANE Select NP_570850.2:p.Lys442=